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Variant : CV594764 (GRCh37/hg19 19p13.11(chr19:17261367-17261718)x1) Homo sapiens

Symbol: CV594764
Name: GRCh37/hg19 19p13.11(chr19:17261367-17261718)x1
Condition: not provided [RCV000740064]
Clinical Significance: benign
Last Evaluated: 09/29/2010
Review Status: no assertion criteria provided
Related Genes: MYO9B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371917,261,367 - 17,261,718CLINVAR
Cytogenetic Map1919p13.11CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14355438
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-14
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.